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Grant: Project Grant

University of British Columbia

$585,224.00

Repurposing slow-release oral morphine as new oral alternative for the treatment of opioid use disorder

EF 2017-18

Résumé
While reversing overdoses with medications like naloxone is a cornerstone of the response to the opioid public health emergency, preventing overdoses through the development of effective treatments for opioid use disorder (OUD) is critical to addressing this epidemic. Unfortunately, in Canada, there are only two proven life-saving treatments: buprenorphine/naloxone (BNX) and methadone. However, these medications have limitations and are not acceptable for many individuals, resulting in a substantial proportion of individuals who remained untreated and at immediate risk of overdose, death and other negative outcomes. Small European studies suggest that slow-release oral morphine (SROM) may be another potentially effective treatment that is better tolerated, and is associated with greater patient satisfaction and reductions in craving compared to methadone. The goal of the proposed research is to build on these encouraging results and rigorously evaluate the relative effectiveness, safety and acceptability of SROM and methadone in real-life clinical settings in Canada. To that end, we will enrol approximately 200 adults with OUD, who are currently exposed to fentanyl, and who have tried but not benefited from treatment with BNX. Eligible participants will be randomized to receive either methadone or SROM for approximately six months, using a double-blind design where neither participants nor their physicians will know which medication they are receiving. Findings from this study will greatly increase our knowledge of the relative benefits of different treatment alternatives for OUD, and how each of them may suit different individuals' needs. Importantly, from a health policy perspective, positive results confirming SROM clinical utility could present significant potential to increase access to an additional form of evidence-based treatment for OUD in Canada, with potential to be scaled up rapidly given that SROM is already available as an inexpensive generic drug.
Programme
Project Grant
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
370136
Name
Fairbairn Nadia S
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Clinical
Prcname2
Behavioural Sciences - B-2
Projecttitle
Repurposing slow-release oral morphine as new oral alternative for the treatment of opioid use disorder
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$585,224
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Methadone; Opioid Agonist Treatment; Opioid Use Disorder; Overdose; Slow-Release Oral Morphine
Abstract
While reversing overdoses with medications like naloxone is a cornerstone of the response to the opioid public health emergency, preventing overdoses through the development of effective treatments for opioid use disorder (OUD) is critical to addressing this epidemic. Unfortunately, in Canada, there are only two proven life-saving treatments: buprenorphine/naloxone (BNX) and methadone. However, these medications have limitations and are not acceptable for many individuals, resulting in a substantial proportion of individuals who remained untreated and at immediate risk of overdose, death and other negative outcomes. Small European studies suggest that slow-release oral morphine (SROM) may be another potentially effective treatment that is better tolerated, and is associated with greater patient satisfaction and reductions in craving compared to methadone. The goal of the proposed research is to build on these encouraging results and rigorously evaluate the relative effectiveness, safety and acceptability of SROM and methadone in real-life clinical settings in Canada. To that end, we will enrol approximately 200 adults with OUD, who are currently exposed to fentanyl, and who have tried but not benefited from treatment with BNX. Eligible participants will be randomized to receive either methadone or SROM for approximately six months, using a double-blind design where neither participants nor their physicians will know which medication they are receiving. Findings from this study will greatly increase our knowledge of the relative benefits of different treatment alternatives for OUD, and how each of them may suit different individuals' needs. Importantly, from a health policy perspective, positive results confirming SROM clinical utility could present significant potential to increase access to an additional form of evidence-based treatment for OUD in Canada, with potential to be scaled up rapidly given that SROM is already available as an inexpensive generic drug.
Competitiondate
201709
Approvedterm2
4 yrs 0 mth
Pinamesdelim
Fairbairn, Nadia S
Approvedterm
4 ans 0 mois
Cihrcontribution2
~ $585,224~ $0~